FDA Inspection
Metalift LlcMetalift Llc – FDA Inspection, Apr 20, 2010
Record Details
This FDA Inspection record concerns Metalift Llc, with an inspection on April 20, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Metalift Llc
- Inspection Date
- April 20, 2010
- Product Type
- Devices
View Company Profile
ID · 59f63455-ce83-4b41-9467-472e63482d97
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 658826
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
7- 21 CFR 820.198(a)General
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
- 21 CFR 803.17Lack of Written MDR Procedures
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